Hardy J - Search Results

1

Widespread sex differences in gene expression and splicing in the adult human brain.

Trabzuni D, Ramasamy A, Imran S, Walker R, Smith C, Weale ME, Hardy J, Ryten M; North American Brain Expression Consortium. Trabzuni D, et al. Among authors: hardy j. Nat Commun. 2013;4:2771. doi: 10.1038/ncomms3771. Nat Commun. 2013. PMID: 24264146 Free PMC article.

2

X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?

Evidente VG, Gwinn-Hardy K, Hardy J, Hernandez D, Singleton A. Evidente VG, et al. Among authors: hardy j. Mov Disord. 2002 Jan;17(1):200-2. doi: 10.1002/mds.1263. Mov Disord. 2002. PMID: 11835466

3

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians.

Subramony SH, Hernandez D, Adam A, Smith-Jefferson S, Hussey J, Gwinn-Hardy K, Lynch T, McDaniel O, Hardy J, Farrer M, Singleton A. Subramony SH, et al. Among authors: hardy j. Mov Disord. 2002 Sep;17(5):1068-71. doi: 10.1002/mds.10241. Mov Disord. 2002. PMID: 12360561

4

Ethnic differences and disease phenotypes.

Hardy J, Singleton A, Gwinn-Hardy K. Hardy J, et al. Science. 2003 May 2;300(5620):739-40. doi: 10.1126/science.300.5620.739. Science. 2003. PMID: 12730580 No abstract available.

5

Genes and parkinsonism.

Hardy J, Cookson MR, Singleton A. Hardy J, et al. Lancet Neurol. 2003 Apr;2(4):221-8. doi: 10.1016/s1474-4422(03)00350-8. Lancet Neurol. 2003. PMID: 12849210 Review.

6

The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases.

Singleton A, Myers A, Hardy J. Singleton A, et al. Among authors: hardy j. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R123-6. doi: 10.1093/hmg/ddh093. Epub 2004 Feb 19. Hum Mol Genet. 2004. PMID: 14976159 Review.

7

Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletion.

Miller DW, Crawley A, Gwinn-Hardy K, Lopez G, Nussbaum R, Cookson MR, Singleton AB, Hardy J, Dogu O. Miller DW, et al. Among authors: hardy j. Neurosci Lett. 2005 Feb 21;374(3):189-91. doi: 10.1016/j.neulet.2004.10.053. Epub 2004 Nov 19. Neurosci Lett. 2005. PMID: 15663960

8

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease.

Fung HC, Chen CM, Hardy J, Hernandez D, Singleton A, Wu YR. Fung HC, et al. Among authors: hardy j. Mov Disord. 2006 Jun;21(6):880-1. doi: 10.1002/mds.20814. Mov Disord. 2006. PMID: 16511860

9

Frontal temporal dementia: dissecting the aetiology and pathogenesis.

Hardy J, Momeni P, Traynor BJ. Hardy J, et al. Brain. 2006 Apr;129(Pt 4):830-1. doi: 10.1093/brain/awl035. Brain. 2006. PMID: 16543401 No abstract available.

10

Genetics of Parkinson's disease and parkinsonism.

Hardy J, Cai H, Cookson MR, Gwinn-Hardy K, Singleton A. Hardy J, et al. Ann Neurol. 2006 Oct;60(4):389-98. doi: 10.1002/ana.21022. Ann Neurol. 2006. PMID: 17068789 Review.

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